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Phase 4 N=44 Randomized Single-blind Treatment

The Effects of BAK on the Blood Aqueous Barrier of Pseudophakic Patients

Dry Eye Syndromes

Enrolled (actual)
44
Serious AEs
0.0%
Results posted
Jul 2012
Primary outcome: Primary: Aqueous Humor Flare — 8.4; 9.3; 11.4; 8.4 photons/msec

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Hydroxypropylmethylcellulose (Drug); Carboxymethylcellulose (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Campinas, Brazil
Primary completion
Dec 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Aqueous Humor Flare
8.4; 9.3; 11.4; 8.4; 11.9; 8.4
SECONDARY
Macular Thickness
258.5; 259.2; 254.9; 256.4; 255.9; 258.3

Summary

BAK is one of the most frequent preservatives in eye drops. BAK is a quaternary ammonium salt with surfactant qualities. It can be bacteriostatic or bactericidal depending on the concentrations used. It has been shown to be effective against most bacteria with a few exceptions, such as Pseudomonas aeruginosa, or picornaviruses. It as been widely used in eyedrops, nose sprays, hand and face washes, mouthwashes, spermicidal creams, and in various other cleaners, sanitizers, and disinfectants. BAK gained popularity when it was first introduced because it also enhances corneal penetration of some drugs by causing epithelial separation. It is present in several ophthalmic formulations, including most of the antiglaucoma medications. If used chronically, BAK has been found to cause ocular surface changes, such as dry eye and punctuate keratitis. BAK has also been suggested to promote a break in the blood aqueous barrier, which may lead to undesirable consequences, such as uveitis and cystoid macular edema. However, this information is controversial. The purpose of this study is to evaluate the consequences of BAK on the blood-retinal and blood-aqueous barriers of pseudophakic patients receiving BAK-preserved lubricating drops.

Eligibility Criteria

Inclusion Criteria

  • Pseudophakic eyes that underwent cataract surgery at least 6 months before.

Exclusion Criteria

  • Use of any eyedrop.
  • Other conditions associated with a break in the blood-aqueous or blood retina barrier (ie diabetes, ARMD, vasculitis, uveitis)
  • Previous history of cystoid macular edema.
  • Previous ocular surgery other than cataract surgery.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01280110). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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